Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders

Author:

Piras Ignazio Stefano1,Costa Anna2,Tirindelli Maria Cristina3,Stoccoro Andrea4ORCID,Huentelman Matthew J1,Sacco Roberto2,Coppedè Fabio4,Lintas Carla2ORCID

Affiliation:

1. Neurogenomics Division, Translational Genomics Research Institute, Phoenix, AZ 85004, USA

2. Service for Neurodevelopmental Disorders, University Campus Bio-Medico, Rome, Italy

3. Hematology Transfusion Medicine, University Campus Bio-Medico, Rome, Italy

4. Medical Genetics Laboratory, Department of Translational Research & New Technologies in Medicine & Surgery, University of Pisa, Pisa, Italy

Abstract

Aim: To assess promoter methylation levels, gene expression levels and 677C>T/1298A>C genotype and allele frequencies of the MTHFR gene in 45 mothers of attention-deficit/hyperactivity disorder affected child/children (ADHDM) and compare it with age matched healthy control mothers (HCM). Materials & methods: High resolution melting analysis, quantitative real time PCR and PCR-RFLP were performed to assess methylation, gene expression and genotyping, respectively. Significance between ADHDM and HCM was assessed by linear (methylation and gene expression) and logistic regression (genotypes). Results: MTHFR gene expression levels were significantly higher in the ADHDM compared with the HCM group (adj-p < 7.7E-04). No differences in MTHFR promoter methylation level and 677C>T/1298A>C genotype frequencies were detected between ADHDM and HCM. Conclusion: We observed increased MTHFR expression levels not resulting from promoter methylation changes in ADHDM respect to HMC, potentially contributing to the ADHD condition in their children and deserving further investigation.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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